Gorham-Stout disease and cerebrospinal fluid otorrhea.

Abstract:

OBJECTIVE AND IMPORTANCE:Gorham-Stout disease is a rare entity characterized by vascular proliferation causing local destruction of bone tissue. Owing to its low incidence and variable clinical presentation, the diagnosis requires a high degree of awareness by the clinician. CLINICAL PRESENTATION:We present the case of a 2-year-old boy diagnosed of Gorham-Stout syndrome with involvement of the temporal bone and secondary cerebrospinal fluid (CSF) leakage. INTERVENTION:Because of the CSF leakage, the patient required two surgical interventions. The second intervention included mastectomy and placement of a patch and a lumbar drainage device during 50 days, after which the leakage ceased. CONCLUSION:Gorham-Stout disease is a rare condition that can affect the skull base and even present with CSF leakage.

journal_name

Pediatr Neurosurg

journal_title

Pediatric neurosurgery

authors

Hernández-Marqués C,Serrano González A,Cordobés Ortega F,Alvarez-Coca J,Sirvent Cerda S,Carceller Lechón F,Azorín Cuadrillero D

doi

10.1159/000336877

subject

Has Abstract

pub_date

2011-01-01 00:00:00

pages

299-302

issue

4

eissn

1016-2291

issn

1423-0305

pii

000336877

journal_volume

47

pub_type

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